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Journal Abstract Search

147 related items for PubMed ID: 4345063

  • 1. Prenatal diagnosis of G M1 -gangliosidosis.
    Lowden JA, Cutz E, Conen PE, Rudd N, Doran TA.
    N Engl J Med; 1973 Feb 01; 288(5):225-8. PubMed ID: 4345063
    [No Abstract] [Full Text] [Related]

  • 2. Intrauterine detection of GM1 gangliosidosis, type 2.
    Booth CW, Gerbie AB, Nadler HL.
    Pediatrics; 1973 Oct 01; 52(4):521-4. PubMed ID: 4742246
    [No Abstract] [Full Text] [Related]

  • 3. Infantile metachromatic leukodystrophy. Confirmation of a prenatal diagnosis.
    Leroy JG, Van Elsen AF, Martin JJ, Dumon JE, Hulet AE, Okada S, Navarro C.
    N Engl J Med; 1973 Jun 28; 288(26):1365-9. PubMed ID: 4707419
    [No Abstract] [Full Text] [Related]

  • 4. [Prenatal diagnosis of Sandhoff's disease (GM2-gangliosidosis, type 2)].
    Harzer K, Stengel-Rutkowski S, Gley EO, Albert A, Murken JD, Zahn V, Henkel KP.
    Dtsch Med Wochenschr; 1975 Jan 17; 100(3):106-8. PubMed ID: 234374
    [Abstract] [Full Text] [Related]

  • 5. Gm-gangliosidosis type I: in utero detection and fetal manifestations.
    Kaback MM, Sloan HR, Sonneborn M, Herndon RM, Percy AK.
    J Pediatr; 1973 Jun 17; 82(6):1037-41. PubMed ID: 4702895
    [No Abstract] [Full Text] [Related]

  • 6. [Prenatal diagnosis of a case of metachromatic leucodystrophy (author's transl)].
    Harzer K, Zahn V, Stengel-Rutkowski S, Gley EO.
    Dtsch Med Wochenschr; 1975 Apr 25; 100(17):951-3. PubMed ID: 1122864
    [Abstract] [Full Text] [Related]

  • 7. Confirmatory studies in the prenatal diagnosis of sphingolipidoses.
    Percy AK, Miller K, Sonneborn M, Kaback MM.
    Pediatr Res; 1973 Oct 25; 7(10):812-7. PubMed ID: 4201091
    [No Abstract] [Full Text] [Related]

  • 8. Prenatal Niemann-Pick disease: biochemical and histologic examination of a 19-gestational week fetus.
    Schneider EL, Ellis WG, Brady RO, McCulloch JR, Epstein CJ.
    Pediatr Res; 1972 Sep 25; 6(9):720-9. PubMed ID: 4643533
    [No Abstract] [Full Text] [Related]

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  • 11. In utero diagnosis of globoid cell leukodystrophy (Krabb's disease).
    Suzuki K, Schneider EL, Epstein CJ.
    Biochem Biophys Res Commun; 1971 Dec 03; 45(5):1363-6. PubMed ID: 5167491
    [No Abstract] [Full Text] [Related]

  • 12. [Prenatal diagnosis of genetic defects].
    Schmid W.
    Schweiz Rundsch Med Prax; 1972 Feb 29; 61(9):290-4. PubMed ID: 5019731
    [No Abstract] [Full Text] [Related]

  • 13. [Clinical, pathological, and biochemical studies in a case of infantile generalized gangliosidosis (G M1 -mucolipidosis]].
    Pfeiffer RA, Diekmann L, Wierich W, von Bassewitz DB, Jünemann G, Damaske E, Werries E, Wässle K.
    Z Kinderheilkd; 1972 Feb 29; 112(1):23-42. PubMed ID: 4259738
    [No Abstract] [Full Text] [Related]

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  • 15. Infantile GM1 gangliosidosis. Histochemical, ultrastructural and biochemical studies.
    Severi F, Magrini U, Tettamanti G, Bianchi E, Lanzi G.
    Helv Paediatr Acta; 1971 Jun 29; 26(2):192-209. PubMed ID: 4257921
    [No Abstract] [Full Text] [Related]

  • 16. [Current data on human amniotic cytology and their significance for medical genetics].
    Brusilovskiĭ AI, Miroshnikova AF.
    Tsitol Genet; 1974 Mar 29; 8(2):169-72. PubMed ID: 4366214
    [No Abstract] [Full Text] [Related]

  • 17. Ganglioside storage diseases.
    O'Brien JS, Okada S, Ho MW, Fillerup DL, Veath ML, Adams K.
    Fed Proc; 1971 Mar 29; 30(3):956-69. PubMed ID: 4252532
    [No Abstract] [Full Text] [Related]

  • 18. Prenatal genetic diagnosis (second of three parts).
    Milunsky A, Littlefield JW, Kanfer JN, Kolodny EH, Shih VE, Atkins L.
    N Engl J Med; 1970 Dec 24; 283(26):1441-7. PubMed ID: 4098222
    [No Abstract] [Full Text] [Related]

  • 19. Animal model: feline GM1 gangliosidosis.
    Baker HJ, Lindsey JR.
    Am J Pathol; 1974 Mar 24; 74(3):649-52. PubMed ID: 4856037
    [No Abstract] [Full Text] [Related]

  • 20. [Case of late infantile form of gangliosidosis G-M1].
    Majdecki T, Ryniewicz B.
    Neurol Neurochir Pol; 1975 Mar 24; 9(2):271-3. PubMed ID: 168506
    [No Abstract] [Full Text] [Related]

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